Disease Directory

Amyotrophic lateral sclerosis type 1 (ALS1) is associated with variants in the SOD1 gene, which can lead to both autosomal dominant and autosomal rece...

Amyotrophic lateral sclerosis type 10 is a form of motor neuron disease that primarily affects the nerve cells responsible for controlling voluntary m...

Amyotrophic lateral sclerosis type 11 (ALS11) is a neurodegenerative condition that primarily affects motor neurons, leading to progressive muscle wea...

Amyotrophic lateral sclerosis type 12 is a form of motor neuron disease that causes progressive weakness and loss of muscle control. It is caused by m...

Amyotrophic lateral sclerosis type 15 is a form of motor neuron disease characterized by progressive deterioration of motor function and, in some case...

Amyotrophic lateral sclerosis type 16 (ALS16) is a neurodegenerative condition that primarily affects the motor system, leading to muscle weakness and...

Amyotrophic lateral sclerosis type 18 is a form of motor neuron disease in which the underlying cause is a mutation in the PFN1 gene. This condition a...

Amyotrophic lateral sclerosis type 19 is an inherited motor neuron disorder that primarily affects movement and respiratory function. It is caused by...

Amyotrophic lateral sclerosis type 2, juvenile is an inherited motor neuron disorder caused by mutations in the ALS2 gene. It primarily affects childr...

Amyotrophic lateral sclerosis type 20 (ALS20) is a form of motor neuron disease caused by a mutation in the HNRNPA1 gene. This condition affects the n...

Amyotrophic lateral sclerosis type 21 is a form of motor neuron disease that primarily affects the neuromuscular system, leading to impairments in mus...

Amyotrophic lateral sclerosis type 22 is a form of motor neuron disease characterized primarily by progressive muscle weakness and loss of motor funct...

Amyotrophic lateral sclerosis type 23 (ALS23) is a genetic condition caused by variants in the ANXA11 gene, inherited in an autosomal dominant manner....

Amyotrophic lateral sclerosis type 3 (ALS3) is characterized by an autosomal dominant inheritance pattern, meaning that a single copy of the mutated g...

Amyotrophic lateral sclerosis type 4 is a neurological condition primarily affecting the motor neurons, leading to progressive muscle weakness and deg...

Amyotrophic lateral sclerosis type 5 is a motor neuron disease caused by mutations in the SPG11 gene. This condition primarily affects the neurons res...

Amyotrophic lateral sclerosis type 6 is a form of a neurodegenerative disorder that primarily affects the motor neurons and leads to progressive muscl...

Amyotrophic lateral sclerosis type 7 is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Amyotrophic lateral sclerosis type 8 is a neurological condition that primarily affects the motor neurons responsible for controlling voluntary muscle...

Amyotrophic lateral sclerosis type 9 (ALS9) is a form of amyotrophic lateral sclerosis caused by mutations in the ANG gene. This condition is inherite...